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Genome Medicine
|
June 5, 2013
Improved coverage and accuracy with strand-conserving sequence enrichment
Toumy Guettouche, Stephan Zuchner
Annals of Neurology
|
September 13, 2016
A novel missense mutation of CMT2P alters transcription machinery
Bo Hu, Sezgi Arpag, Stephan Zuchner, et al.
Human Mutation
|
December 24, 2016
Doublet-Mediated DNA Rearrangement-A Novel and Potentially Underestimated Mechanism for the Formation of Recurrent Pathogenic Deletions
Amir Jahic, Sophie Hinreiner, Werner Emberger, et al.
Handbook of Clinical Neurology
|
February 22, 2023
Peripheral neuropathy in mitochondrial disease
Rita Horvath, Jessica Medina, Mary M Reilly, et al.
Human Mutation
|
July 16, 2015
Innovative genomic collaboration using the GENESIS (GEM.app) platform
Michael Gonzalez, Marni J Falk, Xiaowu Gai, et al.
Stem Cell Research
|
May 26, 2024
Generation of 3 patient induced Pluripotent stem cell lines containing SORD mutations linked to a recessive neuropathy
Christopher Yanick, Renata Maciel, Elizabeth Jacobs, et al.
Clinical and Translational Medicine
|
January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia
David Pellerin, Matt C Danzi, Mathilde Renaud, et al.
Neurology. Genetics
|
February 3, 2026
Expanding the Genetic Landscape of Congenital Insensitivity to Pain
Theeraphong Pho-Iam, Pimchanok Kulsirichawaroj, Surachai Likasitwattanakul, et al.
Nature Communications
|
May 3, 2025
Genetic ancestry and population structure in the All of Us Research Program cohort
Shivam Sharma, Shashwat Deepali Nagar, Priscilla Pemu, et al.
Journal of the Peripheral Nervous System : JPNS
|
October 12, 2022
Conduction block and temporal dispersion in a SIGMAR1-related neuropathy
Rodrigo Siqueira Soares Frezatti, Pedro José Tomaselli, Fernanda Barbosa Figueiredo, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 149) with videos related to
Sort By:
Page
of 15
Genome Medicine
|
June 5, 2013
Improved coverage and accuracy with strand-conserving sequence enrichment
Toumy Guettouche, Stephan Zuchner
Annals of Neurology
|
September 13, 2016
A novel missense mutation of CMT2P alters transcription machinery
Bo Hu, Sezgi Arpag, Stephan Zuchner, et al.
Human Mutation
|
December 24, 2016
Doublet-Mediated DNA Rearrangement-A Novel and Potentially Underestimated Mechanism for the Formation of Recurrent Pathogenic Deletions
Amir Jahic, Sophie Hinreiner, Werner Emberger, et al.
Handbook of Clinical Neurology
|
February 22, 2023
Peripheral neuropathy in mitochondrial disease
Rita Horvath, Jessica Medina, Mary M Reilly, et al.
Human Mutation
|
July 16, 2015
Innovative genomic collaboration using the GENESIS (GEM.app) platform
Michael Gonzalez, Marni J Falk, Xiaowu Gai, et al.
Stem Cell Research
|
May 26, 2024
Generation of 3 patient induced Pluripotent stem cell lines containing SORD mutations linked to a recessive neuropathy
Christopher Yanick, Renata Maciel, Elizabeth Jacobs, et al.
Clinical and Translational Medicine
|
January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia
David Pellerin, Matt C Danzi, Mathilde Renaud, et al.
Neurology. Genetics
|
February 3, 2026
Expanding the Genetic Landscape of Congenital Insensitivity to Pain
Theeraphong Pho-Iam, Pimchanok Kulsirichawaroj, Surachai Likasitwattanakul, et al.
Nature Communications
|
May 3, 2025
Genetic ancestry and population structure in the All of Us Research Program cohort
Shivam Sharma, Shashwat Deepali Nagar, Priscilla Pemu, et al.
Journal of the Peripheral Nervous System : JPNS
|
October 12, 2022
Conduction block and temporal dispersion in a SIGMAR1-related neuropathy
Rodrigo Siqueira Soares Frezatti, Pedro José Tomaselli, Fernanda Barbosa Figueiredo, et al.
Page
of 15